Conceptual Design of Large Surface Area Porous Polymeric Hybrid Media Based on Polyhedral Oligomeric Silsesquioxane Precursors: Preparation, Tailoring of Porous Properties, and Internal Surface Functionalization

被引:84
作者
Alves, Filipa [1 ]
Scholder, Pascal [1 ]
Nischang, Ivo [1 ]
机构
[1] Johannes Kepler Univ Linz, Inst Polymer Chem, A-4060 Leonding, Austria
基金
奥地利科学基金会;
关键词
hierarchical pore structure; hybrid materials; porous properties; nanohybrid building blocks; polyhedral oligomeric silsesquioxane (POSS); thiol-ene "click" chemistry; HIGH-FLOW CHARACTERISTICS; ENE CLICK CHEMISTRY; MEMBRANE SEPARATIONS; MACROPOROUS POLYMERS; NANOBUILDING BLOCKS; HYDROGEN STORAGE; ORGANIC POLYMERS; BUILDING-BLOCKS; CATALYSIS; NANOCOMPOSITES;
D O I
10.1021/am303048y
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
We report on the preparation of hybrid, organic inorganic porous materials derived from polyhedral oligomeric vinylsilsesquioxanes (vinylPOSS) via a single-step molding process. The monolithic, large surface area materials are studied with a particular focus on morphology and porous properties. Radical vinyl polymerization of the nanometer-sized POSS building blocks is therefore utilized via a thermally initiated route and in porogenic diluents such as tetrahydrofuran and polyethylene glycols of varying composition. Careful choice of these porogenic solvents and proper choice of initiator concentration lead to highly porous monolithic building entities which show a rigid, 3D-adhered, porous structure, macroscopically adapting the shape of a given mold. The described materials reflect Brunauer-Emmett-Teller (BET) surface areas of 700 m(2)/g or more and maximum tunable mesopore volumes of up to 2 cm(3)/g. Experimental investigations demonstrate the option to tailor nanoporosity and macroporosity in the single-step free-radical polymerization process. While studies on the influence of the used porogenic solvents reveal tuneability of pore sizes due to the unique pore formation process, tailored existence of residual vinyl groups allows facile postpolymerization modification of the highly porous, large surface area hybrid materials exploited via thiol-ene "click" chemistry. Our developed, simply realizable preparation process explores a new route to derive porous organic-inorganic hybrid adsorbents for a wide variety of applications such as extraction, separation science, and catalysis.
引用
收藏
页码:2517 / 2526
页数:10
相关论文
共 52 条
[1]
Catalysts Immobilized on Organic Polymeric Monolithic Supports: From Molecular Heterogeneous Catalysis to Biocatalysis [J].
Anderson, Emily Baird ;
Buchmeiser, Michael R. .
CHEMCATCHEM, 2012, 4 (01) :30-44
[2]
Photopolymerization kinetics of multifunctional monomers [J].
Andrzejewska, E .
PROGRESS IN POLYMER SCIENCE, 2001, 26 (04) :605-665
[4]
Buchmeiser M.R., 2003, Polymeric materials in organic synthesis and catalysis
[5]
Zeolite membranes - Recent developments and progress [J].
Caro, Juergen ;
Noack, Manfred .
MICROPOROUS AND MESOPOROUS MATERIALS, 2008, 115 (03) :215-233
[6]
Hybrid Porous Materials with High Surface Area Derived from Bromophenylethenyl-Functionalized Cubic Siloxane-Based Building Units [J].
Chaikittisilp, Watcharop ;
Sugawara, Ayae ;
Shimojima, Atsushi ;
Okubo, Tatsuya .
CHEMISTRY-A EUROPEAN JOURNAL, 2010, 16 (20) :6006-6014
[7]
Organic/inorganic hybrid composites from cubic silsesquioxanes. Epoxy resins of octa(dimethylsiloxyethylcyclohexylepoxide) silsesquioxane [J].
Choi, J ;
Yee, AF ;
Laine, RM .
MACROMOLECULES, 2003, 36 (15) :5666-5682
[8]
Recent Developments in the Chemistry of Cubic Polyhedral Oligosilsesquioxanes [J].
Cordes, David B. ;
Lickiss, Paul D. ;
Rataboul, Franck .
CHEMICAL REVIEWS, 2010, 110 (04) :2081-2173
[9]
Ordered porous materials for emerging applications [J].
Davis, ME .
NATURE, 2002, 417 (6891) :813-821
[10]
Aspects of immobilisation of catalysts on polymeric supports [J].
Dioos, Bart M. L. ;
Vankelecom, Ivo F. J. ;
Jacobs, Pierre A. .
ADVANCED SYNTHESIS & CATALYSIS, 2006, 348 (12-13) :1413-1446